The present study is focused on the utilization of naturally occurring abietic acid in the synthesis of high added-value compounds with attractive characteristics. The synthesis of ILs derived from abietic acid was conducted using ion-exchange or neutralization methods, and the products were obtained with high yields exceeding 85%. The study confirmed strong influence of the chemical structure on the physicochemical properties of the obtained compounds, such as solubility, thermal stability, and phase transitions. The results also revealed excellent deterrent properties of ILs with abietate anions toward S. granarius, T. conf usum, and T. granarium, reaching or exceeding the values calculated for azadirachtin. The best results were achieved for cations containing long alkyl substituentstetraalkylammonium and 1-alkyl-3-methylimidazolium cations. Additionally, the obtained compounds exhibited antioxidant properties in the DPPH radical scavenging assay. The highest activity was observed for tetraalkylammonium cations. The obtained results allow for a conclusion that abietate ionic liquids with both antifeedant and antioxidant activity can be successfully implemented into storage crop protection.

a This study was focused on presenting a new class of ionic liquids (ILs) with anions of natural origin. The salts were obtained by hydrolysis of defined triglycerides or edible vegetable oils (coconut oil and canola oil) by quaternary ammonium hydroxides. The basic physicochemical properties of the obtained products were studied and their microbial and deterrent activity was determined. Additionally, their susceptibility to biodegradation was evaluated. The described synthesis pathway utilizes vegetable oils and quaternary ammonium hydroxides as reactants in order to obtain ILs with anions of natural origin, which are characterized by specific biological activity. The majority of the prepared ILs exhibited excellent feeding deterrent properties and could be classified as readily biodegradable compounds. The employed method is characterized by low cost of substrates, high yields and high purity of the obtained products. It might potentially find application as a tool to synthesize environmentally-friendly ILs with attractive properties for a wide range of applications.

A new, cheap and efficient method, which may be used to obtain ILs by modifying commonly used fungicides, is presented.

No abstract

Five bio-ionic liquids (BILs) with choline cations and fatty acid anions derived from pelargonic acid, glycerol tristearate, glycerol trioleate, canola oil, and coconut oil were synthesized and applied as spray adjuvants with three sulfonylurea herbicides: metsulfuron-methyl, iodosulfuron-methyl-sodium, and tribenuron-methyl. Physicochemical properties, including thermal stability, solubility, and surface activity, were determined, and the influence of these BILs on herbicidal efficacy was studied in greenhouse tests using four target weed species: common lambsquarters (Chenopodium album L.), cornflower (Centaurea cyanus L.), corn poppy (Papaver rhoeas L.), and oilseed rape (Brassica napus L.). BILs, particularly those with the oleic anion and anions derived from canola oil and coconut oil, greatly improved herbicidal activity. Addition of BILs to the spray solution significantly reduced the surface tension and contact angle of spray droplets and increased the area of herbicide deposit on the leaf surface.